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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525169Generated: November 1, 2026

Hydrochloric Acid → 5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-4-(3,3'-difluoro-4'-methyl-4-biphenylyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/525169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant3-Fluoro-4-methylbenzeneboronic acidHCID 2782674—
Reactant4-(4-bromo-2-fluorophenyl)-5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 67375886—
CatalystHCID 178418807HCID 178418807—
SolventPotassium CarbonateHCID 11430—
Solvent1,4-DioxaneHCID 31275—
Product5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-4-(3,3'-difluoro-4'-methyl-4-biphenylyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 6826099658%

Reaction Steps

A mixture of 4-(4-bromo-2-fluorophenyl)-5-{[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-one (0.244 mmol), (3-fluoro-4-methylphenyl)boronic acid (0.370 mmol), and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II)-dichloromethane adduct (0.012 mmol) in dioxane (2.0 mL) and 2M aq potassium carbonate (0.5 mL) was irradiated in the microwave at 150° C. for 15 min. The reaction mixture was poured into water (50 mL) and the pH was adjusted to 5 with addition of 1N aq HCl. The aqueous layer was extracted with ethyl acetate (3×50 mL) and the combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Purification of the residue by flash chromatography (100% ethyl acetate) and then reverse phase HPLC (30-65% acetonitrile/water with 0.1% NH4OH) provided the title compound as a tan solid (58%). MS(ES)+ m/e 439.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340529B2
Source datasetuspto-grants-2016_05
ORD IDord-130d4d69d055413f98663949d8e4158d
Source noteuspto-grants-2016_05